Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
  • C08G18/78—Nitrogen
  • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
  • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
  • C08G18/794—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aromatic isocyanates or isothiocyanates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
  • C08G18/022—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing isocyanurate groups
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S521/00—Synthetic resins or natural rubbers -- part of the class 520 series
  • Y10S521/902—Cellular polymer containing an isocyanurate structure

Definitions

• This invention relates to new polymers in particular to new isocyanurate polymers of tolylene diisocyanate.
• compositions of matter comprising from 98.5% to 100% by weight of a polymerised tolylene diisocyanate and from 0% to 1.5% by weight of unpolymerised tolylene diisocyanate, said polymerised tolylene diisocyanate containing at least one isocyanurate ring per molecule and said composition containing from 13.0% to 15.0% free isocyanate groups by weight.
• the is-ocyanurate polymers of the present invention may be made from any of the isomeric tolylene diisocyanates for example tolylene-2:4-diisocyana-te, tolylene-2:6-diisocyanate, tolylene-2:S-diis-ocyanate or mixtures thereof.
• Preferred isocyanurate polymers are those made from tolylene-2:4 diisocyanate, tolylene-2:6 diisocyanate or mixtures of tolylene diisocyanates.
• the isocyanurate polymers of the present invention may be prepared by any of the methods and using any of the catalysts known from the prior art to give isocyanate polymers containing the isocyanurate ring structure.
• the isocyanurate polymer may be prepared by treating the tolylene diisocyanate, either alone or in a suitable solvent with a basic catalyst such as an aliphatic tertiary amine, a basic metallic compound such as an alkali or alkaline earth metal oxide, hydroxide carbonate, alcoholate or phenate, an alkali metal salt of an enolisable compound or a metallic salt of a weak organic carboxylic acid.
• a basic catalyst such as an aliphatic tertiary amine, a basic metallic compound such as an alkali or alkaline earth metal oxide, hydroxide carbonate, alcoholate or phenate, an alkali metal salt of an enolisable compound or a metallic salt of a weak organic carboxylic acid.
• Co-catalys-ts may be used, such as for example mono-N-substituted carbamic esters the use of which in conjunction in conjunction with basic metallic compounds forms the subject of our copending application Serial No. 144,832. It is preferred to use as catalysts, metallic salts of weak organic carboxylic acids optionally in the presence of a mono-N-substituted carbamic ester, such catalysts give considerably reduced polymerisation times.
• Sui-table solvents for use in the preparation of the isocyanurate polymers of the present invention are solvents inert towards isocyanates, and include for example esters such as ethyl acetate, butyl acetate, amyl acetate, diethyl pht-halate, the acetate of the monoethyl ether of ethylene glycol, dimethyl phthalate and butyl benzoate, ketones such as methyl isobutyl ketone, chloroform, benzene, toluene, xylene, sulphur dioxide, butyrolactone, monochlo- 3,280,066 Patented Oct. 18, 1966 robenzene, o-dichlorobenzene, ethers and petroleum ethe-rs or mixture of such solvents.
• esters such as ethyl acetate, butyl acetate, amyl acetate, diethyl pht-halate, the a
• the preparation of the isocyanurate polymer may conveniently be carried out by polymerising the tolylene diisocyanate with a suitable catalyst until the desired polymer has been obtained; further polymerisation may then be prevented for example by mechanical removal of insoluble catalysts by filtration or by the inactivation of soluble catalysts by treatment with the calculated amount, or a slight excess thereof, of a strong acid, such as anhydrous hydrogen chloride or phosphoric acid.
• a strong acid such as anhydrous hydrogen chloride or phosphoric acid.
• the tolylene diisocyanate may be polymerised to a degree such that the required polymer formation has taken place and then after removal or inactivation of catalyst, residual free tolylene diisocyanate may be removed by such processes as extraction, distillation or precipitation of the polymer with a solvent in which the monomeric tolylene diisocyanate is soluble.
• the isocyanurate polymers of tolylene diisocyanate of the present invention are useful in the manufacture of polyurethanes by methods described in the prior art, such polyurethanes may be homogeneous or cellular, rigid or elastomeric. They are particularly useful in the manufacture of polyurethane surface coatings and lacquers in that they possess unique technological properties in giving lacquers having a faster drying rate and possessing superior colour retention to lacquer-s prepared from isocyanurate polymers of a lower mean molecular weight and a higher free tolylene diisocyanate content.
• the isocyanurate polymers of tolylene diisocyanate of the present invention have the added advantage in that possessing a low free tolylene diisocyanate content they present a low toxic hazard to the user, it being well known that volatile diisocyanates such as tolylene diisocyanate constitute a toxic hazard when used for example in applications involving spraying. Especially attractive products with a particularly low toxic hazard are those containing not more than 0.5% of free tolylene diisocyanate.
• Example 1 A mixture of 300 parts 2:4-tolylene diisocyanate, 450 parts ethyl acetate and 0.5 part phenol is stirred under a dry nitrogen atmosphere with exclusion of moisture. The temperature is raised to 55 C. and 3.2 parts of a solution of calcium naphthenate in white spirit containing 4% calcium is added, after which the temperature is maintained at 55 :1" C. for about 13 hours. The catalyst is inactivated by addition of 0.23 part phosphoric acid as a 4% weight/volume solution in ethyl acetate, the resulting pale yellow liquid containing 5. 8% isocyanate groups. This product is finally filtered from a little suspended matter to give a clear pale yellow liquid containing 0.2% free tolylene diisocyanate.
• the product is a solution in ethyl acetate of an isocyanurate polymer of 2:4-tolylene diis-ocyanate containing 14.5% isocyanate groups and 0.5% free tolylene diisocyanate.
• Example 2 0. 6 part of a solution of calcium naphthenate in white spirit containing 4% calcium is added to a mixture of parts 2:4-tolylene diisocyanate and 225 parts ethyl acetate which is stirred under dry nitrogen with exclusion of moisture at 55:1" C. After about 11 hours at this temperature, the isocyanate group content having fallen from 19.3% to about 10.3%, 0.25 part phenol is added and the reaction continued at 55:1" C. for a further 6 /2 hours. The polymerisation is then terminated by the addition of 0.043 part phosphoric acid as a 4% weigh-t/ volume solution in ethyl acetate, after which stirring is continued for a further hour. The resulting pale yellow solution contains 5.9% isocyanate groups, the free 2:4- tolylene diisocyanate content being 0.4%.
• the product is a solution in ethyl acetate of an isocyanurate polymer of tolylene-2:4-diisocyanate containing 14.75% isocyanate groups and 1.0% free tolylene diisocyanate.
• Example 3 A mixture of 1200 parts of mixed 2:4/2z6-tolylenediisocyanate (isomer ratio 80/20), 1800 parts dimethyl phthalate, 2.0 parts of phenol and 8.48 parts of a solution of calcium naphthenate in white spirit containing 4% calcium is stirred under a dry nitrogen atmosphere in the absence of the :moisture. (White spirit is a distilled petroleum fraction boiling at approximately 150- 250 C.) The temperature is raised to 70 C. and the mixture maintained at 70-75 C. for about 22% hours by which time the total isocyanate value of the reaction mixture has fallen to 6.25%. The catalyst is inactivated by the addition of .456 part of phosphoric acid as a 4% weight/ volume solution in dimethyl phthalate.
• the viscous solution of isocyanurate polymer in dimethyl phthalate obtained is diluted with a further 430 parts of dimethyl phthalate and the mixture exaporated to dryness by passing it through an agitated thin film distillation apparatus at 180 C. and a vacuum of 3 to 5 mm. of mercury.
• the white solid powdered residue thus obtained is essentially an isocyanurate polymer of tolylene diisocyanate containing only traces of tolylene diisocycanate and 'dimethyl phthal-ate and analyses at 13.34% total isocyanate groups, less than 0.1% free tolylene diisocyanate and 0.1% dimethyl phthalate.
• the powder is readily soluble in the usual lacquer ester solvents such as ethyl and butyl acetates to give, at 40% concentrations, light yellow liquids having viscosities at C. of between 2 and 4 poises.
• Example 4 A mixture of 300 parts 2:4/2z6-tolylene diisocyanate (isomer ratio 80/20), 450 parts ethyl acetate and 0.5 part phenol is stirred under a nitrogen atmosphere with exclusion of moisture. The temperature is raised to 55 C. and 3.3 parts of a solution of calcium naphthenate in white spirit containing 4% calcium is added, after which the temperature is maintained at 55il C., slight exothermicity being evidenced in the early stages of the polymerisation. When the isocyanate group content of the product has fallen to 5.5% this point being reached in about 14 hours, the catalyst is inactivated by addition of 0.24 part phosphoric acid as a 4% weight/volume solution in ethyl acetate. After filtration from a little suspended matter, the clear pale yellow liquid contains 0.4% free tolylene diisocyanate.
• the product is a solution in ethyl acetate of an isocyanurate polymer of 2:4/2:6-tolylene diisocyanate containing 13.5% isocyanate groups and 1% free tolylene diisocyanate.
• Example 5 150 parts 2:4-tolylene diisocyanate and 225 parts ethyl acetate are successively charged to a reactor previously purged with dry nitrogen. With exclusion of moisture and while maintaining a dry nitrogen atmosphere, the temperature is raised to 55il C. When 0.535 part of a solution of calcium naphthenate in white spirit containing 4% calcium is added. After 15 minutes 0.156 part of a solution of lead naphthenate in white spirit containing 24% lead is added 'and heating continued at 55il C. The slightly exothermic reaction which occurs in about /2 hour is easily controlled, after which heating is continued at 55 :1 C. Four hours after the addition of the lead catalyst 0.25 part phenol is added and heating continued at 55 :1 C.
• the cold product is a clear pale yellow liquid containing 0.2% free tolylene diisocyanate corresponding to an ethyl acetate solution of an isocyanurate polymer of 2:4-tolylene diisocyanate containing 14.5% isocyanate groups and 0.5% free tolylene diisocyanate.
• composition of matter comprising from 98.5% to by weight of a polymerised tolylene diisocyanate and from 0% to 1.5% by weight of unpolymerised tolylene diisocyanate, said polymerised tolylene diisocyanate containing at least one isocyanurate ring per molecule and said composition containing from 13.0% to 15.0% free isocyanate groups by Weight based on the Weight of polymerized and unpolymerized tolylene diisocyanate.
• composition of matter as claimed in claim 1 wherein the polymerised tolylene diisocyanate is selected from the group consisting of polymerised tolylene-2:4-diisocyanat'e, polymerised tolylene-2:6 diisocyanate and polymerised mixed tolylene 2:4- and 2:6-diisocyanates and the tolylene diisocyanate is selected from the group consisting of tolylene-2:4-diisocyanate, tolylene-2:6-diisocyanate and mixed tolylene-2:4- and 2:6-diisocyanates.
• Solutions comprising about 40% composition of matter as claimed in claim 1 and about 60% an organic solvent inert towards the isocyanate group.
• organic solvent is selected from the group consisting of ethyl acetate, butyl acetate, amyi acetate, diethyl phthalate, dimethyl phthalate and butyl benzoate.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Polyurethanes Or Polyureas (AREA)

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Citations (3)

• 0
  • NL NL284111D patent/NL284111A/xx unknown
  • NL NL127062D patent/NL127062C/xx active
  • BE BE623676D patent/BE623676A/xx unknown
• 1961
  • 1961-10-17 GB GB37160/61A patent/GB949253A/en not_active Expired
• 1962
  • 1962-10-15 US US230687A patent/US3280066A/en not_active Expired - Lifetime

Patent Citations (3)

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